Advanced Imaging Research Center, University of Texas Southwestern Medical Center, Dallas, Texas 75390; Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas 75390.
Advanced Imaging Research Center, University of Texas Southwestern Medical Center, Dallas, Texas 75390; Department of Radiology, University of Texas Southwestern Medical Center, Dallas, Texas 75390; Department of Chemistry, University of Texas at Dallas, Richardson, Texas 75080.
J Biol Chem. 2013 May 17;288(20):14488-14496. doi: 10.1074/jbc.M113.461947. Epub 2013 Apr 9.
During hepatic lipogenesis, the glycerol backbone of acylglycerols originates from one of three sources: glucose, glycerol, or substrates passing through the citric acid cycle via glyceroneogenesis. The relative contribution of each substrate source to glycerol in rat liver acylglycerols was determined using (13)C-enriched substrates and NMR. Animals received a fixed mixture of glucose, glycerol, and lactate; one group received [U-(13)C6]glucose, another received [U-(13)C3]glycerol, and the third received [U-(13)C3]lactate. After 3 h, the livers were harvested to extract fats, and the glycerol moiety from hydrolyzed acylglycerols was analyzed by (13)C NMR. In either fed or fasted animals, glucose and glycerol provided the majority of the glycerol backbone carbons, whereas the contribution of lactate was small. In fed animals, glucose contributed >50% of the total newly synthesized glycerol backbone, and 35% of this contribution occurred after glucose had passed through the citric acid cycle. By comparison, the glycerol contribution was ~40%, and of this, 17% of the exogenous glycerol passed first through the cycle. In fasted animals, exogenous glycerol became the major contributor to acylglycerols. The contribution from exogenous lactate did increase in fasted animals, but its overall contribution remained small. The contributions of glucose and glycerol that had passed through the citric acid cycle first increased in fasted animals from 35 to 71% for glucose and from 17 to 24% for glycerol. Thus, a substantial fraction from both substrate sources passed through the cycle prior to incorporation into the glycerol moiety of acylglycerols in the liver.
在肝脂肪生成过程中,酰基甘油的甘油骨架来自三个来源之一:葡萄糖、甘油或通过甘油生成作用经过柠檬酸循环的底物。使用(13)C 标记的底物和 NMR 确定了每种底物源对大鼠肝酰基甘油中甘油的相对贡献。动物接受葡萄糖、甘油和乳酸的固定混合物;一组接受[U-(13)C6]葡萄糖,另一组接受[U-(13)C3]甘油,第三组接受[U-(13)C3]乳酸。3 小时后,收获肝脏以提取脂肪,并通过(13)C NMR 分析水解酰基甘油中的甘油部分。在进食或禁食动物中,葡萄糖和甘油提供了大部分甘油骨架碳,而乳酸的贡献较小。在进食动物中,葡萄糖贡献了新合成的甘油骨架的>50%,其中 35%发生在葡萄糖通过柠檬酸循环之后。相比之下,甘油的贡献约为 40%,其中 17%的外源性甘油首先通过循环。在禁食动物中,外源性甘油成为酰基甘油的主要贡献者。外源性乳酸的贡献确实在禁食动物中增加,但总体贡献仍然较小。在禁食动物中,首先通过柠檬酸循环的葡萄糖和甘油的贡献从 35%增加到 71%,对于甘油从 17%增加到 24%。因此,相当一部分来自两种底物源在掺入肝酰基甘油的甘油部分之前先经过循环。